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Fig. 1 | Clinical Epigenetics

Fig. 1

From: Further refinement of the differentially methylated distant lung-specific FOXF1 enhancer in a neonate with alveolar capillary dysplasia

Fig. 1

Overview in UCSC genome browser of the FOXF1 distant enhancer on chr16q24.1. The newly described and other analyzed ACDMPV-causative deletions are shown as red (maternal deletions) and blue (paternal deletions) bars. The essential segments of Unit 1 on the paternal chr16 [7] and Unit 2 on the maternal chr16 are shown with the blue- and red-dotted rectangles, respectively

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Clinical Epigenetics

ISSN: 1868-7083

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